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    NGS Analysis Software for Clinical Genetics

    Nordlab hyvinvointiyhtymä

    NGS Analysis Software for Clinical Genetics

    1. Planning notice published

      Sep 18, 3:49 AMSeptember 18, 2026 3:49 AM

    2. Questions deadline

      Oct 6, 9:00 AMOctober 6, 2026 9:00 AM

    Brief

    Finland: Tenders/Nordlab hyvinvointiyhtymä/NGS Analysis Software for Clinical Genetics

    Planned

    The competition has not been announced yet.

    Deadline
    Oct 6,Expired
    Agreement
    Buying goods

    Brief

    NordLab is planning the procurement of NGS analytics software for use within its clinical laboratory genetics services, which should support NGS data analysis and interpretation, and enable a high-quality, traceable, and standards-compliant analytical workflow. The software is expected to support the analysis of hereditary diseases, detection of somatic and germline variants, and variant classification and clinical interpretation. The buyer is collecting information to support procurement planning, and suppliers can provide input by responding to this Request for Information (RFI).

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    • Who are you up against?

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    From the notice

    • NordLab is planning the procurement of NGS analytics software for use within its clinical laboratory genetics services. The objective is to gain insight into solutions available on the market, their capabilities, and suppliers' ability to meet current and future needs in clinical diagnostics. The purpose of this Request for Information (RFI) is to collect information to support procurement planning. This RFI is neither a contract notice nor a request for tender and does not obligate the contracting authority to carry out a procurement procedure. The software solution under consideration is intended for clinical use in genetic testing and analysis. The software should support NGS data analysis and interpretation and enable a high-quality, traceable, and standards-compliant analytical workflow. The software is expected to support, among others, the following use cases: Analysis of hereditary diseases Detection of somatic and germline variants Variant classification and clinical interpretation

    • Contact

      Tiina Talalahankinnat@nordlab.fi
    • Type
      Planning
    • Location
      Pohjois-Pohjanmaa
    • Main code
      Medical information systems
      48814000

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